Pharma company: lek
List of lek products:
- 5-Nok
- 5Nok
- Abaktal
- Actobim
- Acyclovir - Pharmacological action Acyclovir Pharma is an antiviral agent. Thymidine kinase of virus-infected cells actively converts acyclovir through a series of sequential reactions in the mono-, di- and triphosphate of acyclovir. The latter interacts with the viral DNA polymerase, and embedded in DNA, which is synthesized for new viruses. Thus it is formed a "defective" viral DNA which leads to suppression of replication of new generations of viruses. This mediciine acyclovir is active against...
- Adavin
- Altramet
- Amlodipine - Amlodipine is a long-acting 1,4-dihydropyridine calcium channel blocker. It acts primarily on vascular smooth muscle cells by stabilizing voltage-gated L-type calcium channels in their inactive conformation. By inhibiting the influx of calcium in smooth muscle cells, amlodipine prevents calcium-dependent myocyte contraction and vasoconstriction. A second proposed mechanism for the drug’s vasodilatory effects involves pH-dependent inhibition of calcium influx via inhibition of smooth...
- Amoksiklav
- Amoksiklav Forte
- Amoksiklav Quick Tabs
- Amoksiklav Quicktabs
- Amoxicillin; Clavulanate
- Amyzol
- Ansilan
- Antopar
- Aprovel - Irbesartan information Irbesartan is a drug that classified as an Angiotensin II receptor antagonist. Irbesartan indications This blood pressure medication (Irbesartan Zydus Pharmaceuticals) is indicated for the treatment of hypertension or high blood pressure. Irbesartan works by preventing the narrowing of blood vessels and arteries and it also prevents the constriction of the flow of blood. Buy Irbesartan Zydus Pharmaceuticals, as it is also prescribed for the treatment of kidney...
- Aprovel Forte - Irbesartan information Irbesartan is a drug that classified as an Angiotensin II receptor antagonist. Irbesartan indications This blood pressure medication (Irbesartan Zydus Pharmaceuticals) is indicated for the treatment of hypertension or high blood pressure. Irbesartan works by preventing the narrowing of blood vessels and arteries and it also prevents the constriction of the flow of blood. Buy Irbesartan Zydus Pharmaceuticals, as it is also prescribed for the treatment of kidney...
- Atorsan
- Biodroxil
- Bromergon
- Bromocriptine - Bromocriptine mesylate is a semisynthetic ergot alkaloid derivative with potent dopaminergic activity. It is indicated for the management of signs and symptoms of Parkinsonian Syndrome. Bromocriptine also inhibits prolactin secretion and may be used to treat dysfunctions associated with hyperprolactinemia. It also causes sustained suppression of somatotropin (growth hormone) secretion in some patients with acromegaly. Bromocriptine has been associated with pulmonary fibrosis. Indication: For...
- Candesartan - Candesartan is an angiotensin-receptor blocker (ARB) that may be used alone or with other agents to treat hypertension. It is administered orally as the prodrug, candesartan cilexetil, which is rapidly converted to its active metabolite, candesartan, during absorption in the gastrointestinal tract. Candesartan lowers blood pressure by antagonizing the renin-angiotensin-aldosterone system (RAAS); it competes with angiotensin II for binding to the type-1 angiotensin II receptor (AT1) subtype and...
- Cefotaxim
- Cimetidine - DESCRIPTION Cimetidine is a histamine H 2 -receptor antagonist. Chemically it is N” -cyano- N -methyl- N’ -[2-[[(5-methyl-1 H -imidazol-4-yl)methyl]thio]-ethyl], guanidine. The molecular formula for cimetidine is C 10 H 16 N 6 S; and the molecular weight is 252.35. The structural formula for cimetidine is: Cimetidine contains an imidazole ring, and is chemically related to histamine. Cimetidine has...
- Cinarizin - Pharmacological action Cinnarizine is a calcium channel blocker class IV with a predominant effect on the brain vessels, a derivative of piperazine. This medication improves cerebral, coronary and peripheral circulation. Cinnarizine violates the entrance of calcium ions into vascular smooth muscle cells. This drug lowers the tone of arteriolar smooth muscle, decreases the vasoconstrictor response to biogenic substances (epinephrine, norepinephrine, bradykinin). Cinnarizine reduces the...
- Cinarizin Forte - Pharmacological action Cinnarizine is a calcium channel blocker class IV with a predominant effect on the brain vessels, a derivative of piperazine. This medication improves cerebral, coronary and peripheral circulation. Cinnarizine violates the entrance of calcium ions into vascular smooth muscle cells. This drug lowers the tone of arteriolar smooth muscle, decreases the vasoconstrictor response to biogenic substances (epinephrine, norepinephrine, bradykinin). Cinnarizine reduces the...
- Ciprolone
- Degan
- Delatar
- Dermazin
- Edicin
- Enalapril - Enalapril information Enalapril is one of the most effective anti-hypertensive drugs in the market. Belonging to the angiotensin-converting-enzyme inhibitors (ACE inhibitors) category of drugs, Enalapril helps to keep raising blood pressure under control thereby reducing the risk factors of this disease. Since hypertension works out the heart muscles to cause early arterial failure, Enalapril stands in the way and helps to keep your heart healthy, indirectly. Like all other ACE inhibitors,...
- Ferrum Lek
- Flexid
- Flonidan
- Fluval
- Immunal
- Kalicor
- Kalijev
- Karvezide
- Ketonal - Pharmacological action Ketoprofen is a NSAID, propionic acid derivative. This medication has analgesic, anti-inflammatory and antipyretic activity. The mechanism of action is associated with inhibition of COX activity - the main enzyme metabolism of arachidonic acid, a precursor of prostaglandins, which play a major role in the pathogenesis of inflammation, pain and fever. A pronounced analgesic effect of ketoprofen is due to two mechanisms: peripheral (indirect, via inhibition of...
- Ketonal Duo - Pharmacological action Ketoprofen is a NSAID, propionic acid derivative. This medication has analgesic, anti-inflammatory and antipyretic activity. The mechanism of action is associated with inhibition of COX activity - the main enzyme metabolism of arachidonic acid, a precursor of prostaglandins, which play a major role in the pathogenesis of inflammation, pain and fever. A pronounced analgesic effect of ketoprofen is due to two mechanisms: peripheral (indirect, via inhibition of...
- Ketonal Forte - Pharmacological action Ketoprofen is a NSAID, propionic acid derivative. This medication has analgesic, anti-inflammatory and antipyretic activity. The mechanism of action is associated with inhibition of COX activity - the main enzyme metabolism of arachidonic acid, a precursor of prostaglandins, which play a major role in the pathogenesis of inflammation, pain and fever. A pronounced analgesic effect of ketoprofen is due to two mechanisms: peripheral (indirect, via inhibition of...
- Ketonal Retard - Pharmacological action Ketoprofen is a NSAID, propionic acid derivative. This medication has analgesic, anti-inflammatory and antipyretic activity. The mechanism of action is associated with inhibition of COX activity - the main enzyme metabolism of arachidonic acid, a precursor of prostaglandins, which play a major role in the pathogenesis of inflammation, pain and fever. A pronounced analgesic effect of ketoprofen is due to two mechanisms: peripheral (indirect, via inhibition of...
- Klimicin
- Kornam
- Kuterid
- Lekamoxiclav
- Lekoklar
- Lekoptin
- Lekoptin Retard
- Lendacin
- Linex
- Lisinopril - WARNING: FETAL TOXICITY • When pregnancy is detected, discontinue lisinopril as soon as possible [see Warnings and Precautions (5.1) ]. • Drugs that act directly on the renin-angiotensin system can cause injury and death to the developing fetus [see ...
- Lomilan
- Lontermin
- Loram - Pharmacological action Lorazepam is an anxiolytic drug (tranquilizer), a derivative of benzodiazepine. This medication has anxiolytic, sedative, hypnotic, anticonvulsant, muscle relaxant central, antiemetic effect. The mechanism of the anxiolytic, sedative and hypnotic action is associated with increased inhibitory effect of GABA in the CNS. Anticonvulsant action, apparently in part due to increased presynaptic inhibition; inhibited the spread of epileptogenic activity arising in the...
- Losartan; Hydrochlorothiazide - This drug is used to treat high blood pressure . It is also used to lower the risk of strokes in patients with high blood pressure and an enlarged heart . Lowering high blood pressure helps prevent strokes, heart attacks , and kidney problems. This product contains two medications: losartan and hydrochlorothiazide . Losartan is an angiotensin receptor blocker and works by relaxing blood vessels so that blood can flow more easily. Hydrochlorothiazide is a "water pill" (diuretic) that...
- Nakom
- Neloren
- Nifecard - Pharmacological action Nifedipine is aSelective calcium channel blocker class II, a derivative of dihydropyridine. This medication inhibits the entry of calcium into cardiomyocytes and vascular smooth muscle cells. Nifedipine has antianginal and hypotensive action. This drug lowers the tone of vascular smooth muscle. Nifedipine dilates coronary and peripheral arteries, lowers blood pressure and slightly - myocardial contractility, reduces afterload and myocardial oxygen demand. This...
- Nifecard XL - Pharmacological action Nifedipine is aSelective calcium channel blocker class II, a derivative of dihydropyridine. This medication inhibits the entry of calcium into cardiomyocytes and vascular smooth muscle cells. Nifedipine has antianginal and hypotensive action. This drug lowers the tone of vascular smooth muscle. Nifedipine dilates coronary and peripheral arteries, lowers blood pressure and slightly - myocardial contractility, reduces afterload and myocardial oxygen demand. This...
- Omeprazole - WARNINGS AND PRECAUTIONS Bone Fracture ( 5.3 ) 09/2010 WARNINGS AND PRECAUTIONS Diminished anti-platelet activity of clopidogrel ( 5.4 ) 01/2011 ...
- Orcal
- Ortanol - Pharmacological action Omeprazole is an inhibitor of H+ K+ ATPase. This medication inhibits the activity of H+-K+-ATPase in gastric parietal cells and thus blocks the final stage of hydrochloric acid secretion. This leads to a reduction in basal and stimulated secretion, regardless of the nature of the stimulus. Due to the reduction of acid secretion omeprazole reduces or normalizes the effects of acid in the esophagus in patients with reflux esophagitis. Omeprazole has a bactericidal...
- Palin
- Portal
- Pravastatin - Pravastatin is a cholesterol-lowering agent that belongs to a class of medications known as statins. It was derived from microbial transformation of mevastatin, the first statin discovered. It is a ring-opened dihydroxyacid with a 6’-hydroxyl group that does not require in vivo activation. Pravastatin is one of the lower potency statins; however, its increased hydrophilicity is thought to confer advantages such as minimal penetration through lipophilic membranes of peripheral cells,...
- Primamet
- Primotren
- Prolekofen
- Pyramil - Ramipril information Ramipril belongs to the class of drugs classified as ACE inhibitors or Angiotensin-Converting-Enzyme inhibitor. Ramipril indications This product is a drug prescribed for the treatment of hypertension or high blood pressure, and for the prevention of heart failures succeeding heart attacks. Ramipril is also used for the prevention of heart attacks, stroke and other heart related problems. Ramipril warnings The medication is major allergen especially to patients...
- Ranital
- Rimstar 4-FDC
- Rispolux - Risperidone information This medication works well for patients suffering from the agonies of bipolar diseases. Mostly, Risperidone helps individuals with schizophrenia and mania. By affecting the functions of different chemicals in the brain, this drug may provide relief to sufferers. However, before using this drug, patients need to be sure about the side effects that may occur. Risperidone can also be used for treating other disorders or as a complementary drug. Risperidone warnings ...
- Rodanol
- Rodanol S
- Roxithromycin - Roxithromycin is a semi-synthetic macrolide antibiotic. It is very similar in composition, chemical structure and mechanism of action to erythromycin, azithromycin, or clarithromycin. Roxithromycin prevents bacteria from growing, by interfering with their protein synthesis. Roxithromycin binds to the subunit 50S of the bacterial ribosome, and thus inhibits the translocation of peptides. Roxithromycin has similar antimicrobial spectrum as erythromycin, but is more effective against certain...
- Sanval
- Tafen
- Tafen Nasal
- Tafen Novolizer
- Tamsulosin - Tamsulosin is a selective antagonist at alpha-1A and alpha-1B-adrenoceptors in the prostate, prostatic capsule, prostatic urethra, and bladder neck. At least three discrete alpha1-adrenoceptor subtypes have been identified: alpha-1A, alpha-1B and alpha-1D; their distribution differs between human organs and tissue. Approximately 70% of the alpha1-receptors in human prostate are of the alpha-1A subtype. Blockage of these receptors causes relaxation of smooth muscles in the bladder neck and...
- Trianol - Pharmacological action Trianol is a medication that violates the synthesis of uric acid. This drug is a structural analog of hypoxanthine. It inhibits the enzyme xanthine oxidase, which is involved in the conversion of hypoxanthine to xanthine and xanthine to uric acid. This is due to decrease in the concentration of uric acid and its salts in body fluids and urine, which helps dissolve existing uric acid deposits and prevents their formation in tissues and kidney. Allopurinol increases...
- Tulip
- Venitan Forte
- Zolpidem - Zolpidem is a prescription short-acting nonbenzodiazepine hypnotic that potentiates gamma-aminobutyric acid (GABA), an inhibitory neurotransmitter, by binding to benzodiazepine receptors which are located on the gamma-aminobutyric acid receptors. Zolpidem is used for the short-term treatment of insomnia. It works quickly (usually within 15 minutes) and has a short half-life (2-3 hours). It is classified as an imidazopyridine. As an anticonvulsant and muscle relaxant, the beneficial effects...
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The information was verified by Dr. Rachana Salvi, MD Pharmacology
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